Prefilled syringe and method of preparing a prefilled syringe

Patent metadata

Field	Value
Publication number	US-12220496-B2
Application number	US-202318330083-A
Country	US
Kind code	B2
Filing date	Jun 6, 2023
Priority date	Sep 29, 2017
Publication date	Feb 11, 2025
Grant date	Feb 11, 2025

Abstract

A method of preparing a prefilled syringe is disclosed that includes obtaining a syringe barrel and a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel and the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel is sterilized by a first sterilizing. Filling a drug substance into an interior of the syringe barrel and sealing the interior of the syringe barrel. Packaging the syringe barrel with a rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel. Providing a second external surface sterilizing of the packaged syringe barrel with the rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel.

First claim

What is claimed is:

1. A prefilled syringe comprising:
a syringe barrel having an open end and a tip with an orifice essentially opposite to the open end;
a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel;
a drug substance arranged in an interior of the syringe barrel; and
a rubber stopper sealing the interior of the syringe barrel,
wherein the rubber element of the needle adaptor cap and the rubber stopper are made of a rubber material having an oxygen transmission rate at 1 atmosphere of not more than 120 cubic centimeter per square meter and day, of between 115 cubic centimeter per square meter and day and 116 cubic centimeter per square meter and day, of not more than 110 cubic centimeter per square meter and day, of not more than 100 cubic centimeter per square meter and day, of not more than 90 cubic centimeter per square meter and day, of not more than 80 cubic centimeter per square meter and day, of not more than 70 cubic centimeter per square meter and day, of not more than 65 cubic centimeter per square meter and day, of between 63 cubic centimeter per square meter and day and 64 cubic centimeter per square meter and day, or of about 63.6 cubic centimeter per square meter and day.

2. A prefilled syringe prepared by a method, comprising the steps of:
obtaining a syringe barrel having an open end and a tip with an orifice essentially opposite to the open end, and a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel, and the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel is sterilized by a first sterilizing comprising a main step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 5 hours to about 60 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C.;
filling a drug substance through the open end of the syringe barrel or through the orifice of the syringe barrel into an interior of the syringe barrel;
sealing the interior of the syringe barrel by advancing a rubber stopper through the open end of the syringe barrel;
packaging the syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel, and
second external surface sterilizing the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel,
wherein
the rubber element of the needle adaptor cap and the rubber stopper are made of a rubber material having an oxygen transmission rate at 1 atmosphere of not more than 120 cubic centimeter per square meter and day, of between 115 cubic centimeter per square meter and day and 116 cubic centimeter per square meter and day, of not more than 110 cubic centimeter per square meter and day, of not more than 100 cubic centimeter per square meter and day, of not more than 90 cubic centimeter per square meter and day, of not more than 80 cubic centimeter per square meter and day, of not more than 70 cubic centimeter per square meter and day, of not more than 65 cubic centimeter per square meter and day, of between 63 cubic centimeter per square meter and day and 64 cubic centimeter per square meter and day, or of about 63.6 cubic centimeter per square meter and day,
the second external surface sterilizing comprises a main step of exposing the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 3 hours to about 30 hours at a relative humidity of about 40% to about 100% and at a temperature of about 25° C. to about 45° C., and
at least one of the duration, the relative humidity and the temperature of the second external surface sterilizing is essentially lower than the respective duration, relative humidity or temperature of the first sterilizing.

3. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the main step of the first sterilizing is performed in a sterilization chamber.

4. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the main step of the first sterilizing comprises exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to a pressure of about 450 millibars to about 1000 millibars.

5. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe in the main step of the first sterilizing, the ethylene oxide is provided in a concentration of about 400 milligrams per liter to about 800 milligrams per liter.

6. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the main step of the first sterilizing comprises flushing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel with air, nitrogen or a combination thereof at a pressure of about 100 millibars or about 200 millibars to about 800 millibars or about 900 millibars after exposing the syringe barrel together with the needle adaptor cap to ethylene oxide.

7. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the first sterilizing comprises a pre-conditioning step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 12 hours to about 96 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C., wherein the pre-conditioning step of the first sterilizing is executed prior the main step of the first sterilizing, wherein the pre-conditioning step of the first sterilizing preferably is performed outside the sterilization chamber.

8. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the first sterilizing comprises a pre-conditioning step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 10 minutes to about 2 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C., wherein the pre-conditioning step of the first sterilizing is executed prior the main step of the first sterilizing, wherein the pre-conditioning step of the first sterilizing preferably is performed inside the sterilization chamber.

9. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the first sterilizing comprises an aeration step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to an air flow for about 12 hours to about 96 hours at a temperature of about 30° C. to about 60° C., wherein the aeration step of the first sterilizing is executed after the main step of the first sterilizing.

10. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the main step of the second external surface sterilizing is performed in a sterilization chamber.

11. The prefilled syringe of claim 2 , wherein in the method of preparing the prefilled syringe the main step of the second external surface sterilizing comprises exposing the packaged syringe barrel together with the rubber stopper

Assignees

• Hoffmann La Roche
• Genentech Inc

Inventors

• Hemminger Markus
• Grauschopf Ulla
• Bamberg Frank
• Bowen Mayumi
• Müller Robert
• Felsovalyi Flora
• Christensen Denny

Classifications

• A61L2103/23

  Containers other than laboratory or medical, e.g. bottles or mail · CPC title

• A61L2103/15

  Laboratory, medical or dentistry appliances, e.g. catheters or sharps · CPC title

• B65B55/02

  Sterilising, e.g. of complete packages · CPC title

• A61M2005/3104

  Caps for syringes without needle · CPC title

• A61M5/31513

  Piston constructions to improve sealing or sliding · CPC title